The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125347452 12534745 2 F 201601 20160627 20160706 20160711 EXP US-TEVA-673151USA TEVA 66.45 YR F Y 63.04000 KG 20160711 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125347452 12534745 1 PS NUVIGIL ARMODAFINIL 1 250 MILLIGRAM DAILY; U 21875 250 MG TABLET QD
125347452 12534745 2 SS NUVIGIL ARMODAFINIL 1 250 MILLIGRAM DAILY; CUTTING THE TABLETS IN HALF U 21875 250 MG TABLET QD
125347452 12534745 3 SS COPAXONE GLATIRAMER ACETATE 1 U 20622 40 MG TIW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125347452 12534745 1 Somnolence
125347452 12534745 3 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125347452 12534745 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125347452 12534745 Blood creatine phosphokinase increased
125347452 12534745 Collagen disorder
125347452 12534745 Condition aggravated
125347452 12534745 Connective tissue disorder
125347452 12534745 Intentional product use issue
125347452 12534745 Metanephrine urine increased
125347452 12534745 Myalgia
125347452 12534745 Normetanephrine urine increased
125347452 12534745 Phaeochromocytoma
125347452 12534745 Spinal disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125347452 12534745 1 2011 0
125347452 12534745 2 2011 0
125347452 12534745 3 1999 0